MSG ingestion has been reported to cause chest pain, facial burning, flushing, paresthesias, sweating, dizziness, headaches, palpitations, nausea, and vomiting in susceptible individuals
Diagnosis
Essential History
Clinical Symptoms
WAO Criteria (2011)
Hypotension in Children
Biphasic Anaphylaxis
Anaphylaxis in which symptoms recur within 1-72 hours (usually within 8-10 hours) after the initial (first phase) symptoms have resolved, despite no further exposure to the trigger
Occurs in up to 23% of adults and up to 11% of children with anaphylaxis
Failing to treat initial symptoms with epinephrine increases risk for biphasic anaphylaxis
Protracted Anaphylaxis
Anaphylaxis episode that lasts hours to days without resolving completely
Seems to be rare
WAO SCIT Systemic Reaction Grading System
Grade 1
2
3
4
5
Symptoms of 1 organ system present:
Cutaneous
Generalized pruritus, urticaria, flushing, or sensation of heat or warmth
Cough perceived to originate in the upper airway, not the lung, larynx, or trachea
OR Conjunctival
Erythema, pruritus or tearing
OR Other
Nausea, metallic taste, or headache
Symptoms >1 organ system present OR Lower respiratory
Asthma: cough, wheezing, shortness of breath (eg, <40% PEF or FEV1 drop, responding to an inhaled bronchodilator)
OR Gastrointestinal
Abdominal cramps, vomiting, or diarrhea
OR Other
Uterine cramps
Lower respiratory
Asthma (eg, 40% PEF or FEV1 drop NOT responding to an inhaled bronchodilator)
OR Upper respiratory
Laryngeal, uvula, or tongue edema with or without stridor
Lower or upper respiratory
Respiratory failure with or without loss of consciousness
OR Cardiovascular
Hypotension with or without loss of consciousness
Death-----
Note
Patients may also have a feeling of impending doom, especially in grades 2, 3, or 4.
In children, behavior changes may be a sign of anaphylaxis; eg, becoming very quiet or irritable and cranky.
Symptoms occurring within the first minutes after the injection may be a sign of severe anaphylaxis; mild symptoms may progress rapidly to severe anaphylaxis and death.
How to Score
The final grade is determined after the event is over
Grade (from table above) includes the following suffixes:
Onset of systemic reaction after injection:
≤5 min - a
>5 to ≤10 min - b
>10 to ≤20 min - c
>20 min - d
and whether epinephrine was not administered:
epinephrine not administered - z
Also include comment regarding initial symptom of systemic reaction and time of onset after injection.
Example grade: "grade 2az; rhinitis; 10 minutes"
If patient's symptoms are not included in the table above or if the differentiation between a true systemic reaction and vasovagal (vasodepressor) reaction is difficult, include comment with grade, as appropriate.
Grading System for Hypersensivity Reactions (Brown)
Lab Testing
Test
Comment
When to draw
Lab details
Total tryptase
(serum, plasma)
Total = mature + pro forms of α/β-tryptases
Schwartz
Peak elevation above baseline 15-60 min after onset of anaphylaxis; declines to baseline with a t1/2 of ∼2 h
Comparing acute and baseline levels improves sensitivity and specificity
Draw within the first 1-3 h after symptom onset if possible; samples collected <15 min or >4 h after symptom onset are less likely to be informative
Fleischer
Serum tryptase t1/2 is 1.5-2 h and peaks post mast cell degranulation in 15-120 minutes
Practice parameter
Levels peak 60-90 min after the onset of anaphylaxis and persist to 6 h
Ideally the measurement should be obtained between 1-2 h after the initiation of symptoms
Castells: some evidence to suggest that rheumatoid factor (IgM) interferes with the tryptase assay to yield falsely elevated levels; newer assays avoid this problem
Elevated tryptase levels may also be seen in renal failure or insufficiency, myocardial infarction, amniotic fluid embolism, SIDS, trauma, certain hematologic disorders (e.g. chronic eosinophilic leukemia, myelodysplastic syndromes, acute leukemias), bone marrow suppression states, chronic helminth infection, any disease causing endogenous stem cell factor elevation, with levels typically <40 ng/mL; 1-3% of healthy population may have tryptase >15 ng/mL
Systemic steroids can suppress tryptase levels to normal range in patients with mastocytosis
Median serum tryptase levels are higher in early infancy (even higher if atopic, median 14.2 mcg/L) and gradually fall to pediatric/adult levels by 9-12 months
Simons: Normal total tryptase levels cannot be used to refute the diagnosis of anaphylaxis because they are seldom increased in patients with food-induced anaphylaxis or those in whom blood pressure remains normal during anaphylaxis
Draw acute level 1-3 h after symptom onset
(Avoid drawing <15 min or >4 h after onset)
Draw baseline level >24 h after symptoms resolved
Phadia AB
Blood can be drawn using normal technique. Collect blood for serum (red top tube) or plasma (tube with heparin, citrate or EDTA). A minimum of 1 mL is required.
Serum or plasma should be placed on ice and frozen as soon as possible. Samples should be shipped frozen by overnight courier if the assay cannot be performed on site.
Mature tryptase
(serum, plasma)
Mature β-tryptase
Peaks 15-60 min after the onset of anaphylaxis and then declines with a t1/2 of ∼2 hours
Total/mature tryptase ratio >20 suggests mastocytosis
As above
Available at VCU
Lawrence B. Schwartz, M.D., Ph.D.
P.O. Box 980263
Richmond, Virginia 23298-0263
Phone: (804) 828-9685
E-mail: lschwart @ vcu.edu
Histamine
(plasma)
Schwartz
Peaks 5-10 min after symptom onset and declines to baseline by 15-30 min
Level may be falsely elevated by drawing blood through a small-bore needle under vacuum or when blood clots (due to basophil histamine release)
Draw as soon as possible after symptom onset: preferably within 15 min; samples collected >30 min after symptom onset are less likely to be informative
Simons
Obtain within 15 minutes to 1 hour of symptom onset; histamine levels peak within 5-15 min of symptom onset and decline to baseline by 60 min
Serum plasma histamine levels that are within normal limits do not rule out the clinical diagnosis of anaphylaxis
In one study, histamine was more sensitive than tryptase in helping to confirm anaphylaxis
As soon as possible after symptom onset, (ideally within 30 min)
Most commercial labs
Pull blood manually (DO NOT use vacuum tubes) under gentle pressure through a 20 gauge or larger needle into a syringe containing either citrate or EDTA.
Should be measured in plasma only (not serum)
The anticoagulated blood should be placed on ice (4 deg C) and centrifuged to separate plasma from cells as soon as possible, and then frozen until ready to be analyzed.
Histamine
(24 h urine collection)
May be elevated up to 24 h after symptom onset; histamine-containing foods and histamine-producing enteric bacteria may raise level
Collection should begin as soon as possible after the acute event
May be helpful if elevated, but normal levels do not exclude mast cell activation
Greenberger: urine histamine levels may be increased even with uvula or tongue angioedema
Level <30 ng/mL considered normal
24 h urine collection starting as soon as possible after symptom onset
N-methylhistamine
(plasma, urine)
Histamine metabolite
May be elevated up to 24 h after symptom onset; histamine-rich foods and histamine-producing enteric bacteria may raise level
Urine level may be helpful if elevated, but normal levels do not exclude mast cell activation
Within 24 hours of symptom onset
May also obtain as 24 h urine collection starting as soon as possible after symptom onset
N-methylimidazole acetic acid
(plasma, urine)
Metabolite of N-methylhistamine
May be elevated up to 24 h after symptom onset; histamine-rich foods and histamine-producing enteric bacteria may raise level
Within 24 hours of symptom onset
Free metanephrine
(plasma)
Elevated in pheochromocytoma, not systemic anaphylaxis
Useful in ruling out a paradoxical response to a pheochromocytoma
Fractionated metanephrines and catecholamines
(24 h urine)
Highly sensitive and specific diagnostic test for pheochromocytoma
Prostaglandin D2
(urine)
Marker of mast cell degranulation
Patients taking NSAIDs for any reason should discontinue them if feasible prior to collection of urine, because NSAIDs block PGD2 synthesis
Reported that some patients with systemic mastocytosis have mast cell activation manifesting as selective excessive release of PGD2 (treatable with NSAIDs but not antihistamines)
24 hour urine, starting at symptom onset
11β-prostaglandin F2α
(urine)
PGD2 metabolite
Patients taking NSAIDs for any reason should discontinue them if feasible prior to collection of urine, because NSAIDs block PGD2 synthesis
24 hour urine, starting at symptom onset
Serotonin
(serum)
Elevated in carcinoid syndrome, not systemic anaphylaxis
5-hydroxyindoleacetic acid, 5-HIAA
(urine)
Serotonin metabolite
Elevated in carcinoid syndrome, not systemic anaphylaxis
Carcinoid tumors release many mediators in an episodic fashion, some of them being also released by mast cells on activation (e.g., histamine, prostaglandins) which partly explains their similar clinical features (flushing, bronchospasm, diarrhea, hypotension) and that they can both respond to antihistamines
24-hour urine preferred because level can vary during the day
Random urine sample along with a urine creatinine level is less sensitive but may be obtained when a 24-hour sample is not feasible
Chromogranin A, CgA (serum)
CgA is a protein found in and released from neuroendocrine cells. Blood CgA level may be elevated in pheochromocytoma and carcinoid syndrome.
Useful to rule out VIP–secreting GI tumor or a medullary carcinoma of the thyroid, which also can secrete vasoactive peptides
Calcitonin level
(serum)
Useful to rule-out medullary thyroid carcinoma
Medullary thyroid carcinoma can cause flushing and diarrhea in patients with advanced disease, at which time they usually also show signs of local involvement and have an increased serum calcitonin level
Standard clinical assay measures total tryptase (sum of pro and mature forms of alpha and beta tryptase) and reflects total mast cell number + mast cell degranulation (assay for mature beta tryptase reflecting pure mast cell degranulation is not available clinically)
Table of Contents
Differential Diagnosis
Other:
Diagnosis
Essential History
Clinical Symptoms
WAO Criteria (2011)
Hypotension in Children
Biphasic Anaphylaxis
Protracted Anaphylaxis
WAO SCIT Systemic Reaction Grading System
Cutaneous
- Generalized pruritus, urticaria, flushing, or sensation of heat or warmth
OR- Angioedema (not laryngeal, tongue or uvular)
ORUpper respiratory
- Rhinitis - (eg, sneezing, rhinorrhea, nasal pruritus and/or nasal congestion)
OR- Throat-clearing (itchy throat)
OR- Cough perceived to originate in the upper airway, not the lung, larynx, or trachea
ORConjunctival
- Erythema, pruritus or tearing
OROther
OR
Lower respiratory
- Asthma: cough, wheezing, shortness of breath (eg, <40% PEF or FEV1 drop, responding to an inhaled bronchodilator)
ORGastrointestinal
- Abdominal cramps, vomiting, or diarrhea
OROther
- Asthma (eg, 40% PEF or FEV1 drop NOT responding to an inhaled bronchodilator)
ORUpper respiratory
- Respiratory failure with or without loss of consciousness
ORCardiovascular
Grading System for Hypersensivity Reactions (Brown)
Lab Testing
(serum, plasma)
(Avoid drawing <15 min or >4 h after onset)
Draw baseline level >24 h after symptoms resolved
(serum, plasma)
P.O. Box 980263
Richmond, Virginia 23298-0263
Phone: (804) 828-9685
E-mail: lschwart @ vcu.edu
(plasma)
(24 h urine collection)
(plasma, urine)
May also obtain as 24 h urine collection starting as soon as possible after symptom onset
(plasma, urine)
(plasma)
(24 h urine)
(urine)
(urine)
(serum)
(urine)
(serum)
Serum Tryptase Levels
Treatment
References